FDA Inspection 927254 — Microfit, Inc.

Microfit, Inc. — FEI 2936523

The FDA completed an inspection of Microfit, Inc. on May 27, 2015 in Fresno, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
May 27, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Fresno, CA (United States)

Citations

IDCFRDescription
1471721 CFR 820.30(g)Design validation - software validation documentation